Now showing items 1-1 of 1

    • Exon-disrupting deletions of NRXN1 in idiopathic generalized epilepsy. 

      Møller, RS; Weber, YG; Klitten, LL; Trucks, H; Muhle, H; Kunz, WS; Mefford, HC; Franke, A; Kautza, M; Wolf, P; Dennig, D; Schreiber, S; Rückert, IM; Wichmann, HE; Ernst, JP; Schurmann, C; Grabe, HJ; Tommerup, N; Stephani, U; Lerche, H; Hjalgrim, H; Helbig, I; Sander, T; EPICURE, Consortium. (2013-02-01)